American Pharmaceutical Review
331 FOLLOWERS
Offers editorial coverage of the latest developments in drug delivery, information technology, research & development, analytical development and control, equipment and facility manufacturing, and regulatory affairs. American Pharmaceutical Review is the leading review journal for business and technology in the pharmaceutical industry throughout North America.
American Pharmaceutical Review
1w ago
Teva Pharmaceuticals International GmbH, a subsidiary of Teva Pharmaceutical Industries Ltd. and mAbxience, a Fresenius Kabi majority-owned group with ..read more
American Pharmaceutical Review
1w ago
Caris Discovery™, the therapeutic research arm of Caris Life Sciences® (Caris), announced a multi-year strategic partnership with Merck KGaA ..read more
American Pharmaceutical Review
1w ago
Ligand Pharmaceuticals announced the launch of Pelthos Therapeutics (Pelthos), a biopharmaceutical company, and the appointment of seasoned industry ..read more
American Pharmaceutical Review
1w ago
ARCA biopharma, Inc. and Oruka Therapeutics announced that they have entered into a definitive agreement to combine the companies in an all-stock ..read more
American Pharmaceutical Review
1w ago
dsm-firmenich, has announced a new strategic collaboration with Oz Medicann Group (OMG) Pharma – an Australian-based biotech innovator in the ..read more
American Pharmaceutical Review
1w ago
The FDA approved Zevtera (ceftobiprole medocaril sodium for injection) for the treatment of adults with Staphylococcus aureus bloodstream infections ..read more
American Pharmaceutical Review
1w ago
Morris & Dickson announced it is the first U.S. distributor of Bavarian Nordic’s newly launched mpox vaccine, JYNNEOS®. As the only FDA-approved mpox ..read more
American Pharmaceutical Review
1w ago
TME Pharma N.V. announced that the US Food and Drug Administration (FDA) has granted Fast Track designation for NOX-A12 (olaptesed pegol), TME Pharma ..read more
American Pharmaceutical Review
1w ago
Charles River Laboratories International, Inc. announced a Good Manufacturing Practice- (GMP) plasmid DNA contract development and manufacturing ..read more
American Pharmaceutical Review
2w ago
The FDA issued an emergency use authorization for Pemgarda (pemivibart) for the pre-exposure prophylaxis (prevention) of COVID-19 in certain adults ..read more